Active substancePerindoprilPerindopril
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  • Dosage form: & nbspPills
    Composition:

    One tablet contains:

    active substance- perindopril erbumine 4 mg, 8 mg;

    Excipients lactose anhydrous 59.33 mg / 118.66 mg, silicon dioxide colloidal anhydrous 0.27 mg / 0.54 mg, microcrystalline cellulose 25,50 mg / 51,00 mg, magnesium stearate 0.90 mg / 1.80 mg .

    Description:Dosage 4 mg: oval tablets, white or almost white, on one side with engraving "D" and on the other side with engravings "5" and "8", separated by a risk. Dosage of 8 mg: round biconvex tablets, white or almost white, on one side with engraving "D" and on the other side with engravings "5" and "9", separated by a risk.
    Pharmacotherapeutic group:Angiotensin-converting enzyme (ACE) inhibitor.
    ATX: & nbsp
  • Perindopril
  • Pharmacodynamics:

    ACE inhibitor (interacts with zinc ions (Zn2+) in the ACE molecule and causes its inactivation). Perindopril acts via its active metabolite perindoprilata. Eliminates the vasoconstrictive effect of angiotensin II, increases the concentration of bradykinin and activates the system of prostaglandins (Pg) (ACE transfers inactive angiotensin I to angiotensin II, which has a vasoconstrictor effect, and also causes degradation of bradykinin and Pg, with vasodilating activity); reduces the production and release of aldosterone, inhibits release of norepinephrine, from the endings of sympathetic nerve fibers and formation of endothelium in the vascular wall. Reduction in the formation of angiotensin II is accompanied by an increase in renin activity of blood plasma (due to inhibition negative feedback). Suppression of ACE is accompanied by an increase activity of both circulating and tissue kallikrein-kinin system, as well as systems Pg. Helps restore the elasticity of large arteries (decrease formation of an excessive amount of subendothelial collagen), reduces the pressure in pulmonary capillaries, with prolonged use reduces the severity myocardial hypertrophy of the left ventricle, and interstitial fibrosis, normalizes isozyme profile of myosin; normalizes the work of the heart. Reduces preload and postnagruzku (reduces systolic and diastolic blood pressure (BP) in the "lying" and "standing"), the filling pressure of the left and right ventricles,general peripheral vascular resistance (OPSS); increases the minute volume of circulation (IOC) and cardiac index, does not increase the frequency of cardiac (HR) in patients with chronic heart failure (CHF), moderately reduces heart rate), increases regional blood flow in muscles. Increases the concentration of high density lipoproteins (HDL), in patients with hyperuricemia reduces the concentration of uric acid. Increases renal.crocus, does not change the rate of glomerular filtration.

    Patients with CHF causes a significant decrease in the severity of clinical signs of heart failure, increases exercise tolerance (according to the veloergometric test), does not reliably decrease blood pressure. After oral administration of the median single dose, the maximum antihypertensive effect is achieved after 4-6 hours and persists for 24 hours. Stabilization of antagonist effect occurs after 1 month of therapy and persists for a long time. The termination of treatment is not accompanied by the development of the "withdrawal" syndrome.Signature: (


    It was found that with the use of perindopril at a dose of 8 mg / day there was a significant decrease in the absolute risk of complications (mortality from cardiovascular diseases,incidence of non-fatal myocardial infarction and / or stopping
    heart with subsequent successful resuscitation).
    Pharmacokinetics:

    Absorption - 25%, bioavailability - 65 - 70%. Eating slows the conversion of perindopril into perindoprilat, thus affecting bioavailability. Therefore, the drug should be taken orally 1 time per day, in the morning, before eating. Time achieve maximum concentration (TCmax)-1 h (perindopril), perindoprilata - 3 -4 hours. Equilibrium concentration (Css) is created on the 4th day. In the process of metabolism 20 % is transformed into an active metabolite - perindoprilat; the rest is in 5 metabolites that do not show pharmacological activity. The half-life (T1/2) Perindopril - 1 h. The relationship between perindoprilat and plasma proteins is insignificant, with an ACE of less than 30% (depends on concentration). The volume of distribution of free perindoprilata is 0.2 l / kg. Perindoprilat is excreted by the kidneys, T1 / 2 of the free metabolite fraction is 3-5 hours.

    The dissociation of perindoprilat, associated with ACE, is slow. As a consequence, the "effective" T1/2 is 25 hours Repeated use of perindopril does not lead to its cumulation, and T1 / 2 perindoprilata with repeated admission corresponds to the period of its activity.

    Excretion of perindoprilat slows in elderly patients, as well as in patients with CHF and> chronic renal failure (CRF) (in the latter, dose adjustment should be performed depending on the creatinine clearance (CC).

    The dialytic clearance of perindopril is 70 ml / min. In patients with cirrhosis, the liver clearance of perindopril is reduced by a factor of 2, while the total amount of perindoprilat formed does not change and correction of the dosing regimen is not required.

    Indications:

    - arterial hypertension;

    - Chronic heart failure;

    stable ischemic heart disease (CHD): a reduction in the risk of cardiovascular complications in patients who have had previous myocardial infarction and / or coronary revascularization.
    Contraindications:

    - hypersensitivity to perindopril, as well as to any other components included in the formulation, or other ACE inhibitors;

    - angioedema in a history as a result of previous therapy with ACE inhibitors, hereditary and / or idiopathic angioedema;

    - lactose intolerance, lactase deficiency or malabsorption syndrome;

    - pregnancy, lactation;

    - age to 18 years (efficacy and safety not established).

    Carefully:

    Care should be taken when application of the drug Perindopril at following conditions: volume reduction circulating blood (BCC) (reception diuretics, salt-free diet, vomiting, diarrhea, hemodialysis), hyponatremia, cerebrovascular diseases, angina pectoris - risk of a sharp decline in blood pressure; Renovascular hypertension, bilateral stenosis of the renal arteries or stenosis of the artery the only kidney is the risk of developing severe arterial hypotension and renal failure; chronic kidney failure; system connective tissue diseases (systemic lupus erythematosus, scleroderma) and immunosuppressant therapy - the risk of agranulocytosis and neutropenia; hyperkalemia; stenosis of the aortic valve, mitral stenosis, atherosclerosis, chronic heart failure (IV functional class by classification NYHA), hypertrophic obstructive cardiomyopathy; during the procedure of hemodialysis from application of high-flow polyacrylonitrile membranes; before the procedure for apheresis of LDL; in patients after kidney transplantation (no an experience clinical application); simultaneously with the desensitizing of therapy allergens; at surgical interference (total anesthesia); the patients with diabetes mellitus receiving hypoglycemic agents for admission inwards or insulin (recommended control concentration of glucose in the blood); intake of potassium-sparing diuretics, potassium preparations, potassium-containing substitutes for edible salt and lithium, hyperkalemia, elderly age, and the use of a negroid race in patients.

    Pregnancy and lactation:

    Relevant controlled studies in pregnant women have not been conducted. Application of the drug Perindopril during pregnancy is contraindicated. ACE inhibitors are able to penetrate the placenta and lead to an increase in the incidence and mortality of the fetus and newborn. The effect of ACE inhibitors on the fetus in the II and III trimesters of pregnancy can lead to fetal development of arterial hypotension, renal insufficiency, deformities of the bones of the skull and face, and even fatal. There are reports of the development of the mother oligohydramnios (expressed decrease in the volume of amniotic fluid), which is due to impaired renal function in the fetus.Oligogidramnion can be accompanied by the appearance of contractures of the upper and lower extremities, deformities of the bones of the skull and face, hypoplastic development of the lungs and slowing of the intrauterine development. In case of pregnancy during treatment with the drug Perindopril, should immediately cancel therapy and, if necessary, prescribe an alternative treatment. If perindopril therapy was performed in the II and / or III trimesters of pregnancy, ultrasound examination of the skull and fetal kidney function should be performed.

    In newborns exposed impact inhibitor ACE in utero, should be conducted careful examination to exclude Arterial hypotension, oliguria and hyperkalemia.

    Currently there are no data on the isolation of perindopril in breast milk. Women receiving Perindopril, should be recommended stop breastfeeding.

    Dosing and Administration:

    Inside, in the morning, before eating.

    If possible, prior to application Perindoprie for patients in the group high risk of developing arterial hypotension should be adjusted BCC.

    Arterial hypertension

    The recommended initial dose is 4 mg once a day, in the morning. When inefficiency of therapy within a month dose can be increased to 8 mg 1 time per day. Perindopril can be used in monotherapy or in combination with other antihypertensive drugs.

    In patients with high renin-angiotensin-aldosterone system (in features in patients with renovascular hypertension following a diet with limited consumption of cookery salt, reduced bcc, decompensation heart failure or severe arterial hypertension) after taking the first dose of the drug may develop marked decrease in blood pressure. Such Patients are advised to start treatment with a dose of 2 mg, under medical supervision.

    At the beginning of drug therapy Perindopril symptomatic arterial hypotension, for prevention which is recommended to stop taking diuretics 2 to 3 days before the estimated initiation of drug therapy Perindopril or use the drug in lower doses of 2 mg once a day (necessary Control of blood pressure, kidney function, content potassium ions in the blood serum). AT then, if necessary, reception diuretics can be resumed.

    In elderly patients, treatment should be started at a dose of 2 mg per day in for 1 week. Then the dose can be increased to 4 mg per day. A month later After starting treatment, the daily dose can be be increased to 8 mg. Dose of the drug increase depending on the clinical effect and function of the kidneys.

    Chronic heart failure

    Treatment of patients with cardiac insufficiency of the drug Perindopril in combination with non-salvage diuretic and / or digoxin and / or beta-adrenoblocker is recommended to begin under careful medical observation, using the drug in the initial dose of 2 mg once a day, in the morning.

    Later, after 2 weeks of treatment in depending on the clinical effect of the dose of the drug can be increased to 4 mg 1 once a day.

    In patients with severe chronic heart failure (IV functional class by classification NYHA) or in patients with risk factors (renal dysfunction and a tendency to violation of water-electrolyte balance, patients simultaneously receiving diuretics and / or vasodilators), treatment It is necessary to conduct a special caution and begin under the careful medical supervision.

    Stable ischemic heart disease (IHD): a reduction in the risk of cardiovascular disease,cardiovascular complications in patients previously after myocardial infarction and / or coronary revascularization With stable ischemic disease heart, the initial dose is 4 mg in for 2 weeks, then the daily dose should be increased to 8 mg (in dependence on kidney function and portability).

    Elderly patients should begin therapy with a dose of 2 mg once daily for one week, then 4 mg once a day in flow next week. Then, taking into account the state of kidney function, the dose should be increased to 8 mg once a day. Increase the dose of the drug only if it is well tolerated in the previously recommended dose.

    Application for renal dysfunction In case of renal insufficiency, dosing is determined by QC: with QC greater than 60 ml / min - 4 mg / day, 30-60 ml / min - 2 mg / day, 15-30 ml / min - 2 mg every other day, below 15 ml / min - 2 mg per day of dialysis (dialysal clearance perindoprilata -70 ml / min).

    Application for violations of liver function In patients with chronic hepatic insufficiency, correction of the dosing regimen is not required.

    Side effects:

    Below is a list of side effects, distributed according to organ systems and frequency of occurrence (classification of the World Health Organization):

    very often - more than 1/10,

    often from more than 1/100 to less than 1/10,

    infrequently - from more than 1/1000 to less than 1/100,

    rarely from more than 1/10000 to less than 1/1000,

    very rarely-from less than 1/10000, including individual messages.

    From the nervous system: often - headache, fatigue, dizziness, decreased appetite, _ tinnitus, visual impairment, convulsions, paresthesia; rarely - lability of mood, insomnia; very rarely confusion.

    From the cardiovascular system: often - excessive reduction of blood pressure and associated symptoms of vasodilation; Very rarely - arrhythmia, angina pectoris, myocardial infarction, stroke (possibly a secondary mechanism of development as a result of a sharp drop in blood pressure), vasculitis.

    On the part of the respiratory system: often - a "dry" cough, difficulty breathing; infrequently - bronchospasm; extremely rarely - eosinophilic pneumonia, rhinitis.

    From the digestive system: often - nausea, vomiting, pain in, abdomen, dysuria, diarrhea or constipation; infrequently - intestinal angioedema; rarely dryness of the oral mucosa; very rarely - cholestatic jaundice, pancreatitis, cytolytic or cholestatic hepatitis.

    Allergic reactions: often - skin rashes, itching; infrequently - hives, angioedema, swelling of the face, extremities, lips, mucous membranes, tongue, epiglottis and / or larynx; very rarely - multiforme exudative erythema.

    From the urinary system: infrequently - decreased kidney function, very, rarely, acute renal failure.

    Other: often - asthenia; rarely - increased sweating, erectile dysfunction.

    Laboratory indicators: often - hypercreatininaemia, proteinuria, hyperkalemia; hyperuricemia; rarely (with prolonged use in high doses) - neutropenia, leukopenia, hypohemoglobinaemia, thrombocytopenia, a decrease in hematocrit; very rarely - agranulocytosis, pancytopenia, increased activity of "liver" transaminases, hyperbilirubinemia, hemolytic anemia (against the background of a deficiency of glucose-6- phosphate dehydrogenase), hypoglycemia.

    Overdose:

    Symptoms: marked decrease in blood pressure, shock, stupor, bradycardia, water-electrolyte disorders, renal failure, hyperventilation, tachycardia, palpitation, dizziness, agitation and cough.

    Treatment: gastric lavage, restoration of the water-electrolyte state, replenishment of the reduced BCC. In the case of a marked decrease in blood pressure, the patient should. take a horizontal position, legs in an elevated position, it is required - intravenous injection of 0.9% sodium chloride solution. Effective hemodialysis (do not use high permeability polyacrylnitrile membranes). Intravenous administration of catecholamines may be required. With the development of bradycardia - atropine, it may be necessary to stage, an artificial pacemaker. It is necessary to constantly monitor the indices of vital fictions and indices of water-electrolyte balance of blood.


    Interaction:

    Diuretics

    In some patients receiving diuretic drugs, especially when excess fluid and / or salts are removed, at the very beginning of perindopril therapy, an excessive decrease in blood pressure can occur.The risk of developing this complication can be reduced by abolishing the diuretic 2-3 days before the start of perindopril therapy, by replenishing the BCC, and by applying an ACE inhibitor at lower doses. Further increase in the dose of the drug should be carried out with caution.

    Potassium-sparing diuretics or potassium preparations, potassium-containing foods and nutritional supplements

    Against the background of therapy with ACE inhibitors decreases the loss of potassium, caused by the intake of diuretic drugs. Simultaneous use of ACE inhibitors and potassium-sparing diuretics (spironolactone, triamterene and amiloride), as well as potassium preparations can lead to a significant increase in potassium in the serum. Use these drugs in combination should be, only in the case of hypokalemia, while it is necessary to observe precautions and regularly monitor the potassium content in the blood serum.

    Lithium

    The simultaneous use of ACE inhibitors and lithium preparations can lead to a reversible increase in the concentration of lithium in the blood plasma and the development of lithium intoxication. Simultaneous use of perindopril and lithium preparations is not recommended.

    Non-steroidal anti-inflammatory drugs (NSAIDs), including high doses of acetylsalicylic acid (more than 3 g / day)

    The use of NSAIDs may be accompanied by a weakening of the antihypertensive effect of% ACE inhibitors; Moreover, it has been established that NSAIDs and ACE inhibitors have an additive effect on the increase in serum potassium, with kidney dysfunction also possible. In some cases, acute renal failure may develop, especially with a decrease in BCC; in elderly patients and with impaired renal function. As a rule, these effects are reversible and are usually observed in patients with impaired renal function.

    Hypotensive drugs

    The antihypertensive effect of perindopril may intensify against a background of simultaneous application with other hypotensive drugs, vasodilators, nitrates of short and prolonged action.

    Insulin and hypoglycemic medicines for oral administration The use of ACE inhibitors in patients with diabetes mellitus may increase the hypoglycemic effect of insulin or sulfonylurea preparations (increased glucose tolerance leads to a decrease in the need for insulin or sulfonylurea preparations).

    Tricyclic antidepressants, agents for general anesthesia

    Simultaneous use of ACE inhibitors and agents for general anesthesia can lead to an increased antihypertensive effect.

    Antipsychotic drugs (antipsychotics)

    Simultaneous use with ACE inhibitors can lead to the development of postural hypotension.

    Sympathomimetics

    May weaken the antihypertensive effect of ACE inhibitors.

    Acetylsalicylic acid as aitiagregantnogo means, thrombolytics, beta-adrenoblockers, nitrates

    Perindopril can be used simultaneously with acetylsalicylic acid, thrombolytic agents, beta-adrenoblockers and / or nitrates.

    Preparations of gold

    With simultaneous use of ACE inhibitors and preparations of gold (sodium aurotomy malate for intravenous use) describes a symptom complex that includes facial flushing, nausea, vomiting and lowering blood pressure.

    Special instructions:

    In the event of an episode of unstable angina during the first month of therapy drug Perindopril in patients with stable ischemic heart disease, it is necessary to evaluate the relationship between the benefit and the risk of continuing therapy with this drug.

    ACE inhibitors can cause a sharp decrease in blood pressure. Symptomatic arterial hypotension is observed rarely in patients without concomitant diseases. The risk of excessive decline AD is higher in patients with reduced BCC (taking diuretics, if you follow a diet with restriction of consumption of cookery salt, with hemodialysis, vomiting, diarrhea, and also in patients with severe degree arterial hypertension with high renin activity of blood plasma). This complication is most typical for patients with severe chronic heart failure as in presence of concomitant renal disease insufficiency, and in its absence (most often this side effect is noted in patients receiving "loop" diuretics in high doses, and also in patients with hyponatremia or with impaired renal function). Have patients at increased risk symptomatic arterial hypotension initiation of therapy should be careful medical supervision. Have patients with ischemic heart disease or with cerebrovascular diseases severe arterial hypotension may lead to the development of myocardial infarction or cerebrovascular complications. AT communication with this treatment of such patients also should start under the medical supervision with further careful titration dose depending on the clinical effect and tolerability.

    Before starting therapy with the drug Perindopril, as well as other inhibitors ACE, as well as during its administration should carefully monitor blood pressure, indicators of kidney function and the content of potassium ions in the blood serum.

    In order to reduce the likelihood of symptomatic arterial hypotension in patients receiving diuretic therapy in high doses, they should be canceled 2-3 days before the drug is started Perindopril. In the future, if necessary, diuretic therapy can be resumed under the close supervision of blood pressure.

    In the case of development of arterial hypotension, the patient should take a horizontal position, if necessary, he should undergo an intravenous infusion with the use of 0.9 % solution of sodium chloride. A marked decrease in blood pressure at the first intake of the drug Perindopril is not a contraindication for its further application. After the recovery of bcc and blood pressure, treatment can be continued provided that the dose of the drug is carefully selected.

    In patients with symptomatic heart failure, arterial hypotension, which may develop in the initial period of therapy with ACE inhibitors, can lead to impaired renal function. In some cases, there has been a reported development of acute renal failure, which is usually is reversible.

    In patients with bilateral stenosis renal artery or stenosis of the artery the only kidney (especially if available renal failure) on the background of therapy ACE inhibitors may increase concentrations of urea and creatinine in blood serum. These changes are usually return to normal after cancellation preparation.

    In some patients with arterial hypertension, if not previously available revealed renal failure, especially with concomitant use diuretic drugs may increase concentration of urea and creatinine in blood serum. These changes are usually are slightly expressed and carry reversible character. In this case it is recommended that the dose be reduced Perindopril and / or cancellation of the diuretic.

    The use of ACE inhibitors in patients with Renovascular Hypertension is accompanied by an increased risk development of severe arterial hypotension and renal insufficiency. Treatment of such patients begin under careful medical supervision using preparation in small doses and further adequate choice of dose. During first few weeks of therapy it is necessary to temporarily stop treatment diuretics and monitor kidney function.

    Anaphylactoid reactions can also develop with the use of inhibitors ACE in patients who underwent apheresis of low density lipoproteins absorption by dextran sulfate or in patients on hemodialysis with high-flow membranes, such as polyacryl nitrile. Therefore, similar combinations should be avoided by applying or other antihypertensive drugs, or alternative membranes for hemodialysis.

    Data on the use of the drug Perindopril after kidney transplantation are absent.

    In the treatment with ACE inhibitors, cases of angioedema, swelling of the face, lips, language, vocal folds and / or larynx, in number of patients who received Perindopril.This complication may occur at any stage of therapy. Edema tongue, vocal cords or larynx may lead to airway obstruction. ways. When a laryngeal whistle appears or angioedema, edema, tongue or vocal cords of the drug Perindopril should be immediately discontinued.

    Emergency therapy includes, In addition to other appointments, immediate subcutaneous injection of epinephrine solution (adrenaline) 1: 1000 (1 mg / ml) 0.3-0.5 ml or slow intravenous administration (in according to the preparation of the infusion solution) under the control of ECG and blood pressure. The patient should be hospitalized for treatment and follow-up for at least 12-24 hours and until the symptoms regress completely.

    In the treatment of ACE inhibitors, cases of angioedema of the intestine are also described. Patients noted abdominal pain (with / without nausea or vomiting); in some cases without a previous angioedema and a normal level of C-1 esterase. The diagnosis was established using computed tomography of the abdominal region, ultrasound examination or at the time of surgery.Symptoms disappeared after discontinuation of ACE inhibitors. Therefore, in patients with abdominal pain taking ACE inhibitors, when establishing a differential diagnosis, it is necessary to consider the possibility of developing angioedema of the intestine.

    Patients who have a history of angioedema, not associated with an ACE inhibitor, may be at increased risk of developing it when treated with drugs of this group.

    Patients receiving ACE inhibitors during desensitizing therapy with Hepaticoptera venom can develop anaphylactoid reactions, life-threatening. By temporarily stopping the use of ACE inhibitors, these reactions could be avoided, but they arose again with the occasional administration of these drugs.

    Very rarely, with the administration of ACE inhibitors, cases of the development of the syndrome, which began with the development of cholestatic jaundice, progressed to fulminant liver necrosis and in some cases resulted in death. The mechanism of development of this syndrome is not clear. Application of the drug Perindopril in patients with signs of jaundice development or a significant increase in the activity of "hepatic" enzymes, it is necessary to cancel and conduct appropriate monitoring of laboratory parameters and the patient's condition.


    There have been cases of development of neutropenia / agranulocytosis, thrombocytopenia and anemia in patients receiving ACE inhibitors. Such cases are quite rare in patients with normal renal function. Neutropenia and agranulocytosis disappear after the withdrawal of ACE inhibitors. Perindopril should be used with extreme caution in patients with systemic vasculitis receiving immunosuppressive therapy, treatment with allopurinol or procainamide, or with combination these risk factors, especially in patients with impaired renal function. In these patients, in some cases, may develop infections that are resistant to antibiotics. In the case of drug use Perindopril these patients should be monitored regularly for blood leukocytes.

    If any symptoms of infection (eg, sore throat, fever) appear, the patient should consult a doctor immediately, as they may be a manifestation of neutropenia.

    It should be borne in mind that in patients of the Negroid race the risk of angioedema development is higher. Like other ACE inhibitors, perindopril is less effective as an antihypertensive drug in patients of the Negroid race. This effect is probably associated with a marked predominance of low-grade status in patients of the Negroid race with arterial hypertension.

    Cough that occurs with the use of inhibitors ACE, is unproductive, persistent and passes after discontinuation treatment. In the differential diagnosis of cough, its possible association with ACE inhibitors should be considered.

    The use of ACE inhibitors in patients, whose condition requires surgical and / or, if necessary, general anesthesia, can lead to the development of arterial hypotension or collapse, which is due to a sharp increase in antihypertensive activity. Should warn surgeon / anesthesiologist about the use of ACE inhibitors and stop taking the drug Perindopril for 24 hours before surgery (including dentistry). With the development of arterial hypotension, it is necessary to maintain blood pressure by replenishing the BCC.

    With the use of ACE inhibitors, it is possible to develop hyperkalemia. Risk factors for hyperkalemia include renal failure, elderly age (over 70 years), diabetes mellitus, concomitant pathological conditions (in particular, a decrease in BCC, acute cardiac decompensation, metabolic acidosis). Giperculosis may cause severe, sometimes fatal cardiac rhythm disturbances. It is recommended to periodically monitor the content of potassium ions in the blood plasma.

    It is usually not recommended to apply Perindopril and potassium preparations, salt substitutes containing potassium ions, potassium-sparing diuretics (spironolactone, triamterene or amiloride) diuretics (spironolactone, triamterene or amiloride) or other drugs associated with risk of increasing the potassium content (eg, heparin) because of the possibility of severe hyperkalemia. If joint intake of these drugs is necessary, then therapy should be accompanied by regular monitoring of potassium in the blood serum. Patients with diabetes may need more careful observation and correction of a dose of hypoglycemic agents for oral and insulin intake,especially during the first month of therapy with an ACE inhibitor, including Perindopril.

    It is not recommended to apply simultaneously with the drug Perindopril lithium preparations.

    Perindopril, like other ACE inhibitors, should be used with caution in patients with obstruction of the left ventricular outflow tract (aortic stenosis, hypertrophic obstructive cardiomyopathy), as well as in patients with mitral stenosis.

    Effect on the ability to drive transp. cf. and fur:

    When using the drug Perindopril Care should be taken when driving a vehicle or doing other work that requires increased attention, especially at the beginning treatment, due to the danger of developing arterial hypotension and dizziness.

    Form release / dosage:

    Tablets 4 mg, 8 mg.

    For 10 tablets in a blister of PVC / PVDC / film and aluminum foil.

    For 3 blisters together with the desiccant (silica gel) is placed in a bag of laminated foil.

    1 package with the instruction for use is placed in a cardboard box.

    Packaging:(10) - blisters (3) - bags from aluminum foil laminated-packs cardboard
    Storage conditions:

    At a temperature of no higher than 25 ° C. Keep out of the reach of children!

    Shelf life:2 years. Do not use after the expiration date.
    Terms of leave from pharmacies:On prescription
    Registration number:LP-001392
    Date of registration:20.12.2011 / 29.08.2013
    Expiration Date:20.12.2016
    The owner of the registration certificate:Aurobindo Pharma Co., Ltd.Aurobindo Pharma Co., Ltd. India
    Manufacturer: & nbsp
    Representation: & nbspAurobindo Pharma, ZAOAurobindo Pharma, ZAO
    Information update date: & nbsp28.08.2015
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